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小鼠性腺分化过程中角蛋白8、18和19的模式:角蛋白19的性别和时间依赖性表达

Patterns of keratins 8, 18 and 19 during gonadal differentiation in the mouse: sex- and time-dependent expression of keratin 19.

作者信息

Appert A, Fridmacher V, Locquet O, Magre S

机构信息

Laboratoire de Physiologie de la Reproduction URA-CNRS 1449, Université Pierre et Marie Curie, Paris, France.

出版信息

Differentiation. 1998 Sep;63(5):273-84. doi: 10.1046/j.1432-0436.1998.6350273.x.

Abstract

The acidic keratins K18 and K19 have been shown to display a sex-specific expression during gonadal differentiation in the rat. To extend these findings, we have undertaken a study of the expression of genes encoding for K18 and K19 and their basic partner K8 in the mouse from 10.5 days of gestation until adulthood, using immunofluorescence, in situ hybridization, and reverse transcriptase polymerase chain reaction (RT-PCR). In the urogenital ridge at 10.5 days of gestation, K18, K19, and K8 are present, in both sexes, in coelomic epithelium in the area of the prospective gonad. At 11 days and 10 h of gestation, they are detected in differentiating gonadal blastema. In male gonads at 11 days and 16 h of gestation the first Sertoli cells differentiate. They are stained for anti-Müllerian hormone by immunofluorescence and appear as dispersed cells throughout the blastema. Progressively, they adhere to each other and form differentiating seminiferous cords. K19 disappears as Sertoli cells differentiate. K18 and K8 continue to be detected in Sertoli cells during fetal life and after birth until 14 days postpartum. In the adult testis, no keratin is observed. In differentiating ovaries, the three keratins are present in somatic cells of the ovigerous cords during fetal life and in primordial follicles differentiating from 1-2 days postpartum. In the course of follicular development, K19 is no longer detected as primordial follicles differentiate into growing follicles. K18 and K18 are present in all stages of follicular development. These results show both differences and similarities with the results previously obtained in the rat. In the mouse, in contrast to the rat, keratins are detected in adult ovaries, and K18 is found in undifferentiated gonads and in ovaries. K18 is, thus, not specific to the testis in the mouse, as it is in the rat. In both species, K19 ceases to be expressed in male gonads as Sertoli cells differentiate and form seminiferous cords. The present observations confirm that downregulation of K19 gene expression in the fetal testis is one of the earliest molecular events attesting the commitment of the undifferentiated gonad to the male differentiative pathway.

摘要

酸性角蛋白K18和K19已被证明在大鼠性腺分化过程中呈现性别特异性表达。为扩展这些研究结果,我们采用免疫荧光、原位杂交和逆转录聚合酶链反应(RT-PCR)技术,对从妊娠10.5天到成年期的小鼠中编码K18、K19及其碱性伴侣K8的基因表达进行了研究。在妊娠10.5天时的泌尿生殖嵴中,K18、K19和K8在两性的未来性腺区域的体腔上皮中均有表达。在妊娠11天10小时时,它们在分化的性腺胚基中被检测到。在妊娠11天16小时的雄性性腺中,第一批支持细胞开始分化。通过免疫荧光法,它们被抗苗勒管激素染色,并在整个胚基中表现为分散的细胞。逐渐地,它们相互黏附并形成分化中的生精索。随着支持细胞的分化,K19消失。在胎儿期和出生后直至产后14天,K18和K8在支持细胞中持续被检测到。在成年睾丸中,未观察到角蛋白。在分化中的卵巢中,在胎儿期的卵索体细胞以及产后1 - 2天开始分化的原始卵泡中,这三种角蛋白均有表达。在卵泡发育过程中,随着原始卵泡分化为生长卵泡,K19不再被检测到。K18和K18在卵泡发育的所有阶段均存在。这些结果显示出与先前在大鼠中获得的结果既有差异又有相似之处。在小鼠中,与大鼠不同的是,在成年卵巢中检测到角蛋白,并且在未分化的性腺和卵巢中发现了K18。因此,在小鼠中,K18不像在大鼠中那样仅特异性地存在于睾丸中。在两个物种中,随着支持细胞分化并形成生精索,雄性性腺中K19的表达均停止。目前的观察结果证实,胎儿睾丸中K19基因表达的下调是最早证明未分化性腺向雄性分化途径定向的分子事件之一。

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